Leocor, Inc. · Class II · Cleared Sep 1, 1992
| K-number | K924110 |
| Device name | LEOCOR CORFLO PUMP -- MODIFICATION |
| Applicant | Leocor, Inc. |
| Product code | DQI |
| Device class | Class II |
| Decision date | Sep 1, 1992 |
| Decision | Substantially Equivalent |
| Regulation | 870.1800 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov